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Description

But general guidelines do exist

Why it was included in the FDA ban While animal studies suggest that DIHEXA may tout these brain benefits (17), the FDA says it has not identified any human exposure data. Meaning: The safety and efficacy of DIHEXA for humans is still up in the air

Once you hit the 6-month period, or 6 total refills, take a break from B12/MIC for a minimum of 3 months

The NDA Filing and the CagriSema FDA Review Timeline Novo Nordisk submitted the NDA on 18 December 2025, formally starting the clock on the CagriSema FDA review